Caenorhabditis elegans as a model for obesity research

被引:73
作者
Zheng, J. [2 ]
Greenway, F. L. [1 ]
机构
[1] Louisiana State Univ Syst, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Louisiana State Univ Agr Ctr, Dept Vet Sci, Baton Rouge, LA USA
基金
美国国家卫生研究院;
关键词
C; elegans; insulin; lipogenesis; serotonin; satiety; oxidation; CHANNEL AQUAPORIN-7 GENE; BARDET-BIEDL-SYNDROME; C-ELEGANS; FAT STORAGE; LIFE-SPAN; ADIPOSE-TISSUE; UNITED-STATES; FOOD-INTAKE; INSULIN; LONGEVITY;
D O I
10.1038/ijo.2011.93
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Caenorhabditis elegans (C. elegans) is a small nematode that conserves 65% of the genes associated with human disease, has a 21-day lifespan, reproductive cycles of 3 days, large brood sizes, lives in an agar dish and does not require committee approvals for experimentation. Research using C. elegans is encouraged and a Caenorhabditis Genetics Center (CGC, Minnesota) is funded by the National Institutes of Health-National Center for Research Resources. Many genetically manipulated strains of C. elegans are available at nominal cost from the CGC. Studies using the C. elegans model have explored insulin signaling, response to dietary glucose, the influence of serotonin on obesity, satiety, feeding and hypoxia-associated illnesses. C. elegans has also been used as a model to evaluate potential obesity therapeutics, explore the mechanisms behind single gene mutations related to obesity and to define the mechanistic details of fat metabolism. Obesity now affects a third of the US population and is becoming a progressively more expensive public health problem. Faster and less expensive methods to reach more effective treatments are clearly needed. We present this review hoping to stimulate interest in using the C. elegans model as a vehicle to advance the understanding and future treatment of obesity. International Journal of Obesity (2012) 36, 186-194; doi:10.1038/ijo.2011.93; published online 10 May 2011
引用
收藏
页码:186 / 194
页数:9
相关论文
共 65 条
[1]  
[Anonymous], 1997, WHO TECHN REP SER
[2]   Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome [J].
Ansley, SJ ;
Badano, JL ;
Blacque, OE ;
Hill, J ;
Hoskins, BE ;
Leitch, CC ;
Kim, JC ;
Ross, AJ ;
Eichers, ER ;
Teslovich, TM ;
Mah, AK ;
Johnsen, RC ;
Cavender, JC ;
Lewis, RA ;
Leroux, MR ;
Beales, PL ;
Katsanis, N .
NATURE, 2003, 425 (6958) :628-633
[3]   Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes [J].
Ashrafi, K ;
Chang, FY ;
Watts, JL ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Ruvkun, G .
NATURE, 2003, 421 (6920) :268-272
[4]  
Ashrafi Kaveh, 2007, WormBook, P1
[5]   A comparative metabolomic study of NHR-49 in Caenorhabditis elegans and PPAR-α in the mouse [J].
Atherton, Helen J. ;
Jones, Oliver A. H. ;
Malik, Shahid ;
Miska, Eric A. ;
Griffin, Julian L. .
FEBS LETTERS, 2008, 582 (12) :1661-1666
[6]   The worm in us -: Caenorhabditis elegans as a model of human disease [J].
Baumeister, R ;
Ge, LM .
TRENDS IN BIOTECHNOLOGY, 2002, 20 (04) :147-148
[7]   Obesity: a time bomb to be defused [J].
Bray, GA .
LANCET, 1998, 352 (9123) :160-161
[8]  
Brey CW, 2009, INT J BIOL SCI, V5, P622
[9]   The Influence of Bacterial Diet on Fat Storage in C. elegans [J].
Brooks, Kyleann K. ;
Liang, Bin ;
Watts, Jennifer L. .
PLOS ONE, 2009, 4 (10)
[10]   IRS-2 pathways integrate female reproduction and energy homeostasis [J].
Burks, DJ ;
de Mora, JF ;
Schubert, M ;
Withers, DJ ;
Myers, MG ;
Towery, HH ;
Altamuro, SL ;
Flint, CL ;
White, MF .
NATURE, 2000, 407 (6802) :377-382